@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_head
{
this:
np:hasAssertion
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_assertion
;
np:hasProvenance
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_provenance
;
np:hasPublicationInfo
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_assertion
a
np:Assertion
.
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_provenance
a
np:Provenance
.
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_assertion
{
miriam-gene:540
a
ncit:C16612
.
lld:C0019202
a
ncit:C7057
.
dgn-gda:DGNee7e3dddca11aff3b3a8d1f3d64599c5
sio:SIO_000628
miriam-gene:540
,
lld:C0019202
;
a
sio:SIO_001121
.
}
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_provenance
{
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_assertion
dcterms:description
"[Wide variations in the clinical phenotype of WD may in part be related to the mutations of the ATP7B genotype, though modifier genes and environmental factors also likely play an important role.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21538285
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP891345.RAw_xMmrf33pJBKHD2Gy6FaoXpS4RGR_GQplY-NMXxUuI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:28+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}